Epigenetic asymmetry in the zygote and mammalian development

被引:51
作者
Feil, Robert [1 ,2 ]
机构
[1] CNRS, UMR 5535, Inst Genet Mol, F-34293 Montpellier, France
[2] Univ Montpellier, F-34059 Montpellier, France
关键词
spermatogenesis; oogenesis; epigenetics; DNA methylation; imprinting; PREIMPLANTATION MOUSE EMBRYOS; BECKWITH-WIEDEMANN-SYNDROME; IMPRINTING CONTROL REGIONS; SILVER-RUSSELL-SYNDROME; DNA METHYLATION; LYSINE METHYLATION; DETERMINES METHYLATION; MATERNAL CHROMATIN; GENE NETWORK; HISTONE H3;
D O I
10.1387/ijdb.082654rf
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In mammals, the maternal and the paternal genome are not functionally equivalent and are both required for embryonic and postnatal development. The genome is organised differently in the oocyte as compared to sperm, in which the DNA is tightly packaged with protamines rather than with histones. The requirement of both the parental genomes for normal development is a consequence of differential epigenetic marking in oogenesis and spermatogenesis, at the regulatory elements that control genomic imprinting. These germ line-derived marks of DNA methylation are resistant to the global waves of demethylation that occur following fertilisation, and bring about the parental allele-specific expression of imprinted genes during development and after birth. Perturbation of the differential organisation of the maternally and paternally derived genomes, before fertilisation, or in the early embryo, can give rise to aberrant growth and developmental disorders in humans.
引用
收藏
页码:191 / 201
页数:11
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